A citation-based method for searching scientific literature

Layla Shahmirzadi, Elizabeth C Chao, Erika Palmaer, Melissa C Parra, Sha Tang, Kelly D Farwell Gonzalez. Genet Med 2014
Times Cited: 74

Yaping Yang, Donna M Muzny, Jeffrey G Reid, Matthew N Bainbridge, Alecia Willis, Patricia A Ward, Alicia Braxton, Joke Beuten, Fan Xia, Zhiyv Niu, Matthew Hardison, Richard Person, Mir Reza Bekheirnia, Magalie S Leduc, Amelia Kirby, Peter Pham, Jennifer Scull, Min Wang, Yan Ding, Sharon E Plon, James R Lupski, Arthur L Beaudet, Richard A Gibbs, Christine M Eng. N Engl J Med 2013
Times Cited: 1195

List of shared articles

Times cited

Exome sequencing in clinical settings: preferences and experiences of parents of children with rare diseases (SEQUAPRE study).
Aline Chassagne, Aurore Pélissier, Françoise Houdayer, Elodie Cretin, Elodie Gautier, Dominique Salvi, Sarah Kidri, Aurélie Godard, Christel Thauvin-Robinet, Alice Masurel,[...]. Eur J Hum Genet 2019

Clinical utility of genomic sequencing.
Matthew B Neu, Kevin M Bowling, Gregory M Cooper. Curr Opin Pediatr 2019

Secondary findings from whole-exome/genome sequencing evaluating stakeholder perspectives. A review of the literature.
J Delanne, S Nambot, A Chassagne, O Putois, A Pelissier, C Peyron, E Gautier, J Thevenon, E Cretin, A L Bruel,[...]. Eur J Med Genet 2019

A retrospective review of multiple findings in diagnostic exome sequencing: half are distinct and half are overlapping diagnoses.
Erica D Smith, Kirsten Blanco, Samin A Sajan, Jesse M Hunter, Deepali N Shinde, Bess Wayburn, Mari Rossi, Jennifer Huang, Cathy A Stevens, Candace Muss,[...]. Genet Med 2019

Genome-Wide Sequencing for Prenatal Detection of Fetal Single-Gene Disorders.
Ignatia B van den Veyver, Christine M Eng. Cold Spring Harb Perspect Med 2015

Ethical Considerations for the Return of Incidental Findings in Ophthalmic Genomic Research.
Emmanuelle Souzeau, Kathryn P Burdon, David A Mackey, Alex W Hewitt, Ravi Savarirayan, Margaret Otlowski, Jamie E Craig.  2016

Patient Decisions to Receive Secondary Pharmacogenomic Findings and Development of a Multidisciplinary Practice Model to Integrate Results Into Patient Care.
J Kevin Hicks, Amy Shealy, Allison Schreiber, Marissa Coleridge, Ryan Noss, Marvin Natowicz, Rocio Moran, Timothy Moss, Angelika Erwin, Charis Eng. Clin Transl Sci 2018

Clinical whole-exome sequencing results impact medical management.
Nancy Niguidula, Christina Alamillo, Layla Shahmirzadi Mowlavi, Zöe Powis, Julie S Cohen, Kelly D Farwell Hagman. Mol Genet Genomic Med 2018

Pediatric Whole Exome Sequencing: an Assessment of Parents' Perceived and Actual Understanding.
Leandra K Tolusso, Kathleen Collins, Xue Zhang, Jennifer R Holle, C Alexander Valencia, Melanie F Myers. J Genet Couns 2017

Whether, when, how, and how much? General public's and cancer patients' views about the disclosure of genomic secondary findings.
Jude Emmanuel Cléophat, Michel Dorval, Zaki El Haffaf, Jocelyne Chiquette, Stephanie Collins, Benjamin Malo, Vincent Fradet, Yann Joly, Hermann Nabi. BMC Med Genomics 2021

Genetic testing in dementia - utility and clinical strategies.
Carolin A M Koriath, Joanna Kenny, Natalie S Ryan, Jonathan D Rohrer, Jonathan M Schott, Henry Houlden, Nick C Fox, Sarah J Tabrizi, Simon Mead. Nat Rev Neurol 2021

Research participants in NGS studies want to know about incidental findings.
Anne Marie Jelsig, Niels Qvist, Klaus Brusgaard, Lilian Bomme Ousager. Eur J Hum Genet 2015